Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.55443725T>ACA356914971CLOCK,TMEM165c.1864A>T (p.Met622Leu)
n.31A>T
c.353-8514T>A
n.446A>T
c.409-8514T>A
c.899-8514T>A (n.899-8514T>A)
c.1687A>T (p.Met563Leu)
4g.55443725T>CCA2925795CLOCK,TMEM165c.1864A>G (p.Met622Val)
n.31A>G
c.353-8514T>C
n.446A>G
c.409-8514T>C
c.899-8514T>C (n.899-8514T>C)
c.1687A>G (p.Met563Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.55443725T>GCA356914961CLOCK,TMEM165c.1864A>C (p.Met622Leu)
n.31A>C
c.353-8514T>G
n.446A>C
c.409-8514T>G
c.899-8514T>G (n.899-8514T>G)
c.1687A>C (p.Met563Leu)
4g.55443725T=CA1459075117CLOCK,TMEM165c.1864A= (p.Met622=)
n.31A=
c.353-8514T=
n.446A=
c.409-8514T=
c.899-8514T= (n.899-8514T=)
c.1687A= (p.Met563=)
4g.55443726G>ACA439485115CLOCK,TMEM165c.1863C>T (p.His621=)
n.30C>T
c.353-8513G>A
n.445C>T
c.409-8513G>A
c.899-8513G>A (n.899-8513G>A)
c.1686C>T (p.His562=)
4g.55443726G>CCA356914975CLOCK,TMEM165c.1863C>G (p.His621Gln)
n.30C>G
c.353-8513G>C
n.445C>G
c.409-8513G>C
c.899-8513G>C (n.899-8513G>C)
c.1686C>G (p.His562Gln)
4g.55443726G>TCA356914980CLOCK,TMEM165c.1863C>A (p.His621Gln)
n.30C>A
c.353-8513G>T
n.445C>A
c.409-8513G>T
c.899-8513G>T (n.899-8513G>T)
c.1686C>A (p.His562Gln)
4g.55443727T>ACA356914983CLOCK,TMEM165c.1862A>T (p.His621Leu)
n.29A>T
c.353-8512T>A
n.444A>T
c.409-8512T>A
c.899-8512T>A (n.899-8512T>A)
c.1685A>T (p.His562Leu)
4g.55443727T>CCA356914986CLOCK,TMEM165c.1862A>G (p.His621Arg)
n.29A>G
c.353-8512T>C
n.444A>G
c.409-8512T>C
c.899-8512T>C (n.899-8512T>C)
c.1685A>G (p.His562Arg)
4g.55443727T>GCA356914990CLOCK,TMEM165c.1862A>C (p.His621Pro)
n.29A>C
c.353-8512T>G
n.444A>C
c.409-8512T>G
c.899-8512T>G (n.899-8512T>G)
c.1685A>C (p.His562Pro)
4g.55443728G>ACA356914993CLOCK,TMEM165c.1861C>T (p.His621Tyr)
n.28C>T
c.353-8511G>A
n.443C>T
c.409-8511G>A
c.899-8511G>A (n.899-8511G>A)
c.1684C>T (p.His562Tyr)
4g.55443728G>CCA2925796CLOCK,TMEM165c.1861C>G (p.His621Asp)
n.28C>G
c.353-8511G>C
n.443C>G
c.409-8511G>C
c.899-8511G>C (n.899-8511G>C)
c.1684C>G (p.His562Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443728G=CA1459075119CLOCK,TMEM165c.1861C= (p.His621=)
n.28C=
c.353-8511G=
n.443C=
c.409-8511G=
c.899-8511G= (n.899-8511G=)
c.1684C= (p.His562=)
4g.55443728G>TCA356914999CLOCK,TMEM165c.1861C>A (p.His621Asn)
n.28C>A
c.353-8511G>T
n.443C>A
c.409-8511G>T
c.899-8511G>T (n.899-8511G>T)
c.1684C>A (p.His562Asn)
4g.55443729C>ACA356915003CLOCK,TMEM165c.1860G>T (p.Gln620His)
n.27G>T
c.353-8510C>A
n.442G>T
c.409-8510C>A
c.899-8510C>A (n.899-8510C>A)
c.1683G>T (p.Gln561His)
4g.55443729C>GCA356915004CLOCK,TMEM165c.1860G>C (p.Gln620His)
n.27G>C
c.353-8510C>G
n.442G>C
c.409-8510C>G
c.899-8510C>G (n.899-8510C>G)
c.1683G>C (p.Gln561His)
4g.55443729C>TCA439485121CLOCK,TMEM165c.1860G>A (p.Gln620=)
n.27G>A
c.353-8510C>T
n.442G>A
c.409-8510C>T
c.899-8510C>T (n.899-8510C>T)
c.1683G>A (p.Gln561=)
4g.55443730T>ACA356915005CLOCK,TMEM165c.1859A>T (p.Gln620Leu)
n.26A>T
c.353-8509T>A
n.441A>T
c.409-8509T>A
c.899-8509T>A (n.899-8509T>A)
c.1682A>T (p.Gln561Leu)
4g.55443730T>CCA356915008CLOCK,TMEM165c.1859A>G (p.Gln620Arg)
n.26A>G
c.353-8509T>C
n.441A>G
c.409-8509T>C
c.899-8509T>C (n.899-8509T>C)
c.1682A>G (p.Gln561Arg)
4g.55443730T>GCA356915021CLOCK,TMEM165c.1859A>C (p.Gln620Pro)
n.26A>C
c.353-8509T>G
n.441A>C
c.409-8509T>G
c.899-8509T>G (n.899-8509T>G)
c.1682A>C (p.Gln561Pro)
4g.55443731G>ACA356915025CLOCK,TMEM165c.1858C>T (p.Gln620Ter)
n.25C>T
c.353-8508G>A
n.440C>T
c.409-8508G>A
c.899-8508G>A (n.899-8508G>A)
c.1681C>T (p.Gln561Ter)
4g.55443731G>CCA96904593CLOCK,TMEM165c.1858C>G (p.Gln620Glu)
n.25C>G
c.353-8508G>C
n.440C>G
c.409-8508G>C
c.899-8508G>C (n.899-8508G>C)
c.1681C>G (p.Gln561Glu)
 dbSNP
4g.55443731G=CA1459075121CLOCK,TMEM165c.1858C= (p.Gln620=)
n.25C=
c.353-8508G=
n.440C=
c.409-8508G=
c.899-8508G= (n.899-8508G=)
c.1681C= (p.Gln561=)
4g.55443731G>TCA356915029CLOCK,TMEM165c.1858C>A (p.Gln620Lys)
n.25C>A
c.353-8508G>T
n.440C>A
c.409-8508G>T
c.899-8508G>T (n.899-8508G>T)
c.1681C>A (p.Gln561Lys)
4g.55443732A=CA1459075126CLOCK,TMEM165c.1857T= (p.Thr619=)
n.24T=
c.353-8507A=
n.439T=
c.409-8507A=
c.899-8507A= (n.899-8507A=)
c.1680T= (p.Thr560=)
4g.55443732A>CCA439485123CLOCK,TMEM165c.1857T>G (p.Thr619=)
n.24T>G
c.353-8507A>C
n.439T>G
c.409-8507A>C
c.899-8507A>C (n.899-8507A>C)
c.1680T>G (p.Thr560=)
4g.55443732A>GCA2925797CLOCK,TMEM165c.1857T>C (p.Thr619=)
n.24T>C
c.353-8507A>G
n.439T>C
c.409-8507A>G
c.899-8507A>G (n.899-8507A>G)
c.1680T>C (p.Thr560=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.55443732A>TCA439485125CLOCK,TMEM165c.1857T>A (p.Thr619=)
n.24T>A
c.353-8507A>T
n.439T>A
c.409-8507A>T
c.899-8507A>T (n.899-8507A>T)
c.1680T>A (p.Thr560=)
4g.55443733G>ACA356915046CLOCK,TMEM165c.1856C>T (p.Thr619Ile)
n.23C>T
c.353-8506G>A
n.438C>T
c.409-8506G>A
c.899-8506G>A (n.899-8506G>A)
c.1679C>T (p.Thr560Ile)
4g.55443733G>CCA356915049CLOCK,TMEM165c.1856C>G (p.Thr619Ser)
n.23C>G
c.353-8506G>C
n.438C>G
c.409-8506G>C
c.899-8506G>C (n.899-8506G>C)
c.1679C>G (p.Thr560Ser)
4g.55443733G>TCA356915057CLOCK,TMEM165c.1856C>A (p.Thr619Asn)
n.23C>A
c.353-8506G>T
n.438C>A
c.409-8506G>T
c.899-8506G>T (n.899-8506G>T)
c.1679C>A (p.Thr560Asn)
4g.55443734T>ACA356915061CLOCK,TMEM165c.1855A>T (p.Thr619Ser)
n.22A>T
c.353-8505T>A
n.437A>T
c.409-8505T>A
c.899-8505T>A (n.899-8505T>A)
c.1678A>T (p.Thr560Ser)
4g.55443734T>CCA356915063CLOCK,TMEM165c.1855A>G (p.Thr619Ala)
n.22A>G
c.353-8505T>C
n.437A>G
c.409-8505T>C
c.899-8505T>C (n.899-8505T>C)
c.1678A>G (p.Thr560Ala)
4g.55443734T>GCA356915067CLOCK,TMEM165c.1855A>C (p.Thr619Pro)
n.22A>C
c.353-8505T>G
n.437A>C
c.409-8505T>G
c.899-8505T>G (n.899-8505T>G)
c.1678A>C (p.Thr560Pro)
4g.55443735T>ACA439485127CLOCK,TMEM165c.1854A>T (p.Thr618=)
n.21A>T
c.353-8504T>A
n.436A>T
c.409-8504T>A
c.899-8504T>A (n.899-8504T>A)
c.1677A>T (p.Thr559=)
 gnomAD v4
4g.55443735T>CCA439485128CLOCK,TMEM165c.1854A>G (p.Thr618=)
n.21A>G
c.353-8504T>C
n.436A>G
c.409-8504T>C
c.899-8504T>C (n.899-8504T>C)
c.1677A>G (p.Thr559=)
4g.55443735T>GCA439485129CLOCK,TMEM165c.1854A>C (p.Thr618=)
n.21A>C
c.353-8504T>G
n.436A>C
c.409-8504T>G
c.899-8504T>G (n.899-8504T>G)
c.1677A>C (p.Thr559=)
4g.55443736G>ACA356915068CLOCK,TMEM165c.1853C>T (p.Thr618Ile)
n.20C>T
c.353-8503G>A
n.435C>T
c.409-8503G>A
c.899-8503G>A (n.899-8503G>A)
c.1676C>T (p.Thr559Ile)
4g.55443736G>CCA356915069CLOCK,TMEM165c.1853C>G (p.Thr618Arg)
n.20C>G
c.353-8503G>C
n.435C>G
c.409-8503G>C
c.899-8503G>C (n.899-8503G>C)
c.1676C>G (p.Thr559Arg)
4g.55443736G=CA1459075129CLOCK,TMEM165c.1853C= (p.Thr618=)
n.20C=
c.353-8503G=
n.435C=
c.409-8503G=
c.899-8503G= (n.899-8503G=)
c.1676C= (p.Thr559=)
4g.55443736G>TCA2925798CLOCK,TMEM165c.1853C>A (p.Thr618Lys)
n.20C>A
c.353-8503G>T
n.435C>A
c.409-8503G>T
c.899-8503G>T (n.899-8503G>T)
c.1676C>A (p.Thr559Lys)
 dbSNP ExAC gnomAD v2
4g.55443737T>ACA356915079CLOCK,TMEM165c.1852A>T (p.Thr618Ser)
n.19A>T
c.353-8502T>A
n.434A>T
c.409-8502T>A
c.899-8502T>A (n.899-8502T>A)
c.1675A>T (p.Thr559Ser)
4g.55443737T>CCA356915076CLOCK,TMEM165c.1852A>G (p.Thr618Ala)
n.19A>G
c.353-8502T>C
n.434A>G
c.409-8502T>C
c.899-8502T>C (n.899-8502T>C)
c.1675A>G (p.Thr559Ala)
4g.55443737T>GCA356915074CLOCK,TMEM165c.1852A>C (p.Thr618Pro)
n.19A>C
c.353-8502T>G
n.434A>C
c.409-8502T>G
c.899-8502T>G (n.899-8502T>G)
c.1675A>C (p.Thr559Pro)
4g.55443738G>ACA439485132CLOCK,TMEM165c.1851C>T (p.Gly617=)
n.18C>T
c.353-8501G>A
n.433C>T
c.409-8501G>A
c.899-8501G>A (n.899-8501G>A)
c.1674C>T (p.Gly558=)
4g.55443738G>CCA439485133CLOCK,TMEM165c.1851C>G (p.Gly617=)
n.18C>G
c.353-8501G>C
n.433C>G
c.409-8501G>C
c.899-8501G>C (n.899-8501G>C)
c.1674C>G (p.Gly558=)
4g.55443738G>TCA439485134CLOCK,TMEM165c.1851C>A (p.Gly617=)
n.18C>A
c.353-8501G>T
n.433C>A
c.409-8501G>T
c.899-8501G>T (n.899-8501G>T)
c.1674C>A (p.Gly558=)
4g.55443739C>ACA356915083CLOCK,TMEM165c.1850G>T (p.Gly617Val)
n.17G>T
c.353-8500C>A
n.432G>T
c.409-8500C>A
c.899-8500C>A (n.899-8500C>A)
c.1673G>T (p.Gly558Val)
 gnomAD v4
4g.55443739C>GCA356915086CLOCK,TMEM165c.1850G>C (p.Gly617Ala)
n.17G>C
c.353-8500C>G
n.432G>C
c.409-8500C>G
c.899-8500C>G (n.899-8500C>G)
c.1673G>C (p.Gly558Ala)
4g.55443739C>TCA356915085CLOCK,TMEM165c.1850G>A (p.Gly617Asp)
n.17G>A
c.353-8500C>T
n.432G>A
c.409-8500C>T
c.899-8500C>T (n.899-8500C>T)
c.1673G>A (p.Gly558Asp)

Number of alleles fetched